Device recall
Z-2922-2020: Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is…
FDA device recall · Class II · TELEFLEX MEDICAL INC
Key facts
| Recall number (Z-number) | Z-2922-2020 |
|---|---|
| Recall event | 86200 |
| Product | Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical procedure requiring attachment to a Chest Drainage device. The thoracic catheter is indicated for use less than 30 days. |
| Product code | GBX |
| Recalling firm | TELEFLEX MEDICAL INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 14, 2023 |
| FEI number | 3005747797 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database